In-Situ Freeze Dryers Automatic Device Use Medicine Pharmacy Biological Research

A benchtop automatic freeze-drying (lyophilization) device designed for pharmaceutical and biological research. It performs controlled freezing and sublimation to preserve sensitive materials and is offered in multiple models (HXLG-20FD, HXLG-20F, HXLG-20FT, HXLG-50F).

Typical uses include pharmaceutical R&D, lyophilized drug and reagent preparation, biological sample preservation (proteins, peptides, vaccines, tissues, cells), laboratory experiments requiring freeze-drying, and quality control in drug manufacturing.

The device carries CE marking and ISO9001 certification, indicating compliance with applicable European safety requirements and a certified quality management system. For regulatory compliance in your region, check local requirements and supplier documentation.

The product is listed as a Class IIIB instrument in the manufacturer's specifications, indicating its classification level for performance and intended use. Verify how this classification maps to your local medical/device regulatory categories before clinical or regulated use.

The specification lists the power source as 'Other.' Exact electrical requirements depend on the selected model and regional configuration; confirm voltage, frequency, and plug type with the supplier or in the technical datasheet before purchase and installation.

The unit is described as automatic and user-friendly. It supports automated freeze-drying cycles (controlled freezing, primary and secondary drying). Specific control interfaces and programmable cycle features vary by model—refer to the model datasheet or contact support for UI details and training options.

Single package size is 56 x 45 x 45 cm and single gross weight is 12.000 kg. These indicate a compact benchtop footprint, but final installed footprint and clearances should be checked in the product manual.

Model choice depends on throughput needs, sample types, and any feature differences (e.g., tray configuration or temperature ranges). Contact the vendor or review detailed model datasheets for condenser capacity, shelf area, cycle automation features and any model-specific specs.

Designed for a wide range of lab and pharmaceutical samples including aqueous solutions, biologicals (proteins, enzymes, vaccines), small tissue samples and formulations for lyophilization. Maximum sample volume and number of vials/shelves depend on the chosen model—refer to the model specifications.

Routine maintenance typically includes defrosting/cleaning the condenser, checking vacuum pump oil (if an external pump is used), inspecting seals and valves, and cleaning shelves and product-contact surfaces per manufacturer instructions. Follow the supplied maintenance schedule and keep records for regulated environments.

Yes—online technical support is available as stated in the product description. For on-site installation, training, spare parts or validation documentation, contact the supplier or authorized service representative.

Follow standard laboratory safety: use appropriate PPE, handle infectious or hazardous materials in a suitable containment area (biosafety cabinet) before loading, ensure proper ventilation, and decontaminate the chamber and accessories as required. Consult the device manual and your institution's biosafety officer for specific procedures.

The device is intended for pharmaceutical research and lab use. For regulated production, IQ/OQ/PQ and qualification documentation will be required. Contact the manufacturer for validation protocols, calibration certificates and documentation to support GMP or other regulatory requirements.

Contact the vendor or authorized distributor for spare parts, consumables (seals, valves, trays), and warranty terms. The manufacturer provides online technical support; they will supply part numbers, lead times and service/warranty details.